SE-ATLAS

Neurogenic scapuloperoneal syndrome, Kaeser type Botulism Autosomal dominant proximal spinal muscular atrophy Genetic periodic paralysis Congenital myasthenic syndrome Periodic paralysis with transient compartment-like syndrome Intellectual disability-developmental delay-contractures syndrome Andersen-Tawil syndrome Macrophagic myofasciitis Poliomyelitis Neuromuscular disease Juvenile primary lateral sclerosis Distal myopathy Infantile-onset X-linked spinal muscular atrophy Infantile-onset ascending hereditary spastic paralysis Myotonic syndrome Potassium-aggravated myotonia Thomsen and Becker disease Periodic paralysis Proximal spinal muscular atrophy Bulbospinal muscular atrophy Immune-mediated acquired neuromuscular junction disease Postpoliomyelitis syndrome Monomelic amyotrophy Muscular tumor Cyprus facial-neuromusculoskeletal syndrome Infectious, fungal or parasitic myopathy Primary lateral sclerosis Idiopathic camptocormia Muscular dystrophy-white matter spongiosis syndrome Progressive muscular atrophy Amyotrophic lateral sclerosis type 4 Idiopathic dropped head syndrome Madras motor neuron disease Scapuloperoneal spinal muscular atrophy Vacuolar myopathy with sarcoplasmic reticulum protein aggregates Amyotrophic lateral sclerosis Muscular channelopathy Isaacs syndrome Morvan syndrome Muscular dystrophy Spinal muscular atrophy-progressive myoclonic epilepsy syndrome Hypokalemic periodic paralysis Skeletal muscle disease Distal hereditary motor neuropathy Hyperkalemic periodic paralysis Paramyotonia congenita of Von Eulenburg Genetic skeletal muscle disease Juvenile amyotrophic lateral sclerosis Acquired skeletal muscle disease Idiopathic inflammatory myopathy Malignant hyperthermia of anesthesia Neuromuscular junction disease Genetic neuromuscular junction disease Tel Hashomer camptodactyly syndrome Acquired neuromuscular junction disease Non-dystrophic myopathy Motor neuron disease Genetic motor neuron disease Myotonia permanens Myotonia fluctuans Acquired motor neuron disease Acetazolamide-responsive myotonia